Binnaz Yalcin

22PUBLICATIONS
172CO-AUTHORS
Genome structure and regulationEpigenetics (incl. genome methylation and epigenomics)Adolescent healthCellular nervous systemNeurology and neuromuscular diseases
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Publications (22)

|Jun 26, 2026
RBMX functional retrocopy safeguards brain development in a species-dependent context.

|Mar 30, 2026
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

Ilaria Parenti, Alina Hesters, Marta Gil-Salvador

|Jan 12, 2026
Proceedings of the 12th International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related Disorders.

Fabrizio Vacca, Binnaz Yalcin, Lars Kaestner

|Jan 06, 2026
CRISPR knockout screens reveal genes and pathways essential for neuronal differentiation and implicate PEDS1 in neurodevelopment.

Alana Amelan, Stephan C Collins, Nadirah S Damseh

|Nov 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Ghayda M Mirzaa, Keqin Yan, Raissa Relator

|Nov 28, 2024
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome.

Efil Bayam, Peggy Tilly, Stephan C Collins

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Frequent Collaborators

5 joint publications

Stephan C Collins

5 joint publications

Christopher J Lelliott

3 joint publications

William Dobyns

3 joint publications

Alfredo Brusco